Instructions for Use
Bodystik
Serial no.: xx|8|301|yyy and 2301xxxxx
Page 20
Version: 7 | Release date: 02. August 2021
Any changes to Bodystik, in particular unauthorised
modifications, are prohibited.
The Bodystik is not intended for the control of vital physiological
parameters where the nature of the change could lead to
immediate danger to the patient, e.g. changes in heart function,
respiration or central nervous system activity.
Any other than the described use is deemed improper use.
The responsible organisation of Bodystik alone is liable for any
damage resulting from not adhering to these conditions.
Intended use also includes complying with all further information
and instructions in this IFU, without exception.
Attention
Electromagnetic compatibility (EMC) in accordance with
DIN EN 60601-1-2:2016-05; VDE 0750-1-2:2016-05; IEC 60601-1-
2:2014. See chap. 12.4 “Electromagnetic Compatibility / EMC
Guidelines”. Bodystik is suitable for use in all institutions including
those in residential areas and those which are directly connected to
the public supply network which also supplies buildings used for
residential purposes.
